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Toitu of America, Inc.

2 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
TOITU FETAL ACTOCARDIOGRAPH, MT-332 (K894036)Toitu of America, Inc.1989-11-06
TOITU DOPPLER FETUS DETECTOR, FD-400D (K890139)Toitu of America, Inc.1989-03-29

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Every clearance here is in the API, with alerts when new ones post.